|Publication number||US7182227 B2|
|Application number||US 10/475,911|
|Publication date||Feb 27, 2007|
|Filing date||Apr 29, 2002|
|Priority date||Apr 27, 2001|
|Also published as||DE60205367D1, DE60205367T2, EP1392582A2, EP1392582B1, US20040149780, WO2002087976A2, WO2002087976A3|
|Publication number||10475911, 475911, PCT/2002/1906, PCT/GB/2/001906, PCT/GB/2/01906, PCT/GB/2002/001906, PCT/GB/2002/01906, PCT/GB2/001906, PCT/GB2/01906, PCT/GB2001906, PCT/GB2002/001906, PCT/GB2002/01906, PCT/GB2002001906, PCT/GB200201906, PCT/GB201906, US 7182227 B2, US 7182227B2, US-B2-7182227, US7182227 B2, US7182227B2|
|Inventors||Steven Poile, Geoffrey Robert Hammond, Malcolm Tom McKechnie|
|Original Assignee||Reckitt Bencklser (Uk) Limited|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (12), Referenced by (53), Classifications (6), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The present invention provides an aerosol delivery system driven by hydrostatic pressure from an osmotic or hydrogel swelling device.
The use of aerosol delivery systems for the delivery of active agents is well known for a broad range of applications from personal care to surface cleaning to air perfuming. Conventional aerosol delivery systems rely upon hydrostatic pressure being introduced to the device during manufacture to enable expulsion of the contents upon demand during use. Generally such hydrostatic pressure has been applied by the introduction of gaseous propellants under pressure during manufacture, for example air or butane. The disadvantage of such systems is that the internal pressure decreases as the system is used, reducing the delivery rate of the active agents. There can also be problems when inflammable propellants are used. Furthermore the manufacturing process is expensive because of the pressurised product. A solution to these problems has been sought.
According to the invention there is provided an aerosol delivery system comprising a container defining a chamber for a product to be delivered, an outlet from the chamber through which product may in operation be delivered, a valve for controlling passage of product through the outlet and a pump for pressurising product to be delivered, wherein the pump comprises an expandable material which, in operation, may be expanded to provide the pressure for pressurising product to be delivered, the expandable material being an osmotically effective agent and/or a swellable hydrogel, and being disposed on one side of a semi-permeable membrane through which, in operation, fluid may be absorbed by the expandable material to expand it and thereby generate an osmotic pressure.
The expandable material may apply pressure to the active agent via either an impermeable membrane or a piston.
Suitable materials for use as the swellable hydrogel include polymeric materials optionally blended homogeneously or heterogeneously with osmotically effective agents. The polymeric material is optionally of plant, animal or synthetic origin. The material interacts with water or a biological fluid by absorbing the water or fluid and swelling or expanding to an equilibrium state. The polymeric material preferably exhibits the ability to retain a significant fraction of imbibed fluid in its polymeric molecular structure.
Preferably the polymeric material is a gel polymer that can swell or expand to a very high degree; for example it can have a 2- to 50-fold volume increase. A suitable gel polymer is a swellable, hydrophilic polymer (or an osmopolymer) which is optionally either non-cross-linked or lightly cross-linked. The cross-links can be covalent, ionic or hydrogen bonds so that the polymer possesses the ability to swell in the presence of fluid but does not dissolve in the fluid.
A polymeric material suitable for use in the expandable member is, for example, a poly(hydroxyalkylmethacrylate) having a molecular weight of from 5,000 to 5,000,000; poly(vinyl pyrrolidone) having a molecular weight of from 10,000 to 360,000; an anionic and/or cationic hydrogel; a poly(electrolyte) complex; poly(vinyl alcohol) having a low acetate residual; a swellable mixture of agar and carboxymethyl cellulose; a swellable composition comprising methyl cellulose mixed with a sparingly cross-linked agar; a water-swellable copolymer produced by a dispersion of finely divided copolymer of maleic anhydride with styrene, ethylene, propylene or isobutylene; a water-swellable polymer of N-vinyl lactams; or a swellable sodium salt of carboxymethyl cellulose.
Alternatively, the polymeric material could be a gelable, fluid-imbibing and -retaining polymer such as a pectin having a molecular weight ranging from 30,000 to 300,000; a polysaccharide such as agar, acacia, karaya, tragacenth, algins and guar; an acidic carboxy polymer or its salt derivative such as one sold under the trade name Carbopol; a polyacrylamide; a water-swellable indene maleic anhydride polymer; a polyacrylic acid having a molecular weight of 80,000 to 200,000 such as one sold under the trade name Good-rite; a polyethylene oxide polymer having a molecular weight of 100,000 to 5,000,000 such as one sold under the trade name Good-rite; a starch graft copolymer; an acrylate polymer with water absorbability of about 400 times its original weight such as one sold under the trade name Aqua-Keep; a diester of polyglucan; a mixture of cross-linked poly(vinyl alcohol) and poly (N-vinyl 2 pyrrolidone); or poly(ethylene glycol) having a molecular weight of 4,000 to 100,000.
Other suitable polymer materials for use as the expandable member are those disclosed in U.S. Pat. Nos. 3,865,108, 4,002,173, 4,207,893, 4,220,152, 4,327,725 and 4,350, 271, all of which are incorporated herein by reference, and in Scott et al, Handbook of Common Polymers, CRC Press, Cleveland, Ohio (1971).
The osmotically effective agent is in general an osmotically effective solute which is soluble in fluid imbibed into the expandable member such that there is an osmotic pressure gradient across the semi-permeable membrane against the fluid source. A suitable osmotically effective agent is, for example, magnesium sulphate, magnesium chloride, sodium chloride, lithium chloride, potassium chloride, potassium sulphate, sodium sulphate, sodium phosphate (including hydrates thereof), mannitol, urea, sorbitol, inositol, sucrose, dextrose, lactose, fructose, glucose, magnesium succinate, sodium carbonate, sodium sulphite, sodium bicarbonate, potassium acid phthalate, calcium bicarbonate, potassium acid phosphate, raffinose, tartaric acid, succinic acid, calcium lactate or mixtures thereof. The osmotic pressure in atmospheres (atm) of the osmotically effective agents suitable for use in the invention must be greater than zero atm, generally from 8 atm up to 500 atm, or higher.
The solution of the osmotically effective agent exhibits an osmotic pressure gradient against the fluid source, and is preferably a saturated aqueous salt solution. To maintain the solution saturated and therefore to achieve a constant osmotic pressure throughout operation of the dispenser, the expandable member containing the solution also contains an excess of the osmotically effective agent in solid form. The amount of the excess osmotically effective agent depends on the size of the system and the amount of product to be delivered. The excess solid can be in the form of dispersed particles or, preferably, in the form of a pellet. The solution can initially be a solution of the same or of an osmotically effective agent different from the solid excess agent.
The semi-permeable membrane is permeable to water but impermeable to the osmotically effective compound. Examples of suitable semi-permeable membranes include semi-permeable homopolymers or copolymers. For example, the semi-permeable membrane is based on a cellulose ester, cellulose monoester, cellulose diester, cellulose triester, cellulose ether, cellulose ester ether; mono-, di- and tri-cellulose alkanylate; mono-, di- and tri alkenylate; and/or mono-, di- and tri-aroylate. Suitable examples of cellulose esters include cellulose acylate, cellulose diacylate, cellulose triacylate, cellulose acetate, cellulose diacetate and cellulose triacetate.
The cellulose polymers suitable for use as the semi-permeable membrane have a degree of substitution (D.S.) on their anhydroglucose unit from greater than zero to three. The “degree of substitution” is the average number of hydroxyl groups originally present on the anhydroglucose unit which have been replaced by a substituting group or converted into another group.
The anhydroglucose unit can be partially or completely substituted with groups such as acyl, alkanoyl, aroyl, alkyl, alkenyl, alkoxyl, halogen, carboalkyl, alkylcarbamate, alkylcarbonate, alkylsulfonate, and other semi-permeable polymer forming groups which would be known to a person of skill in the art.
A suitable polymer for use as the semi-permeable membrane includes a cellulose acetate having a D.S. of 1.8 to 2.3 and an acetyl content of 32% to 39.9%; cellulose diacetate having a D.S. of 1 to 2 and an acetyl content of 21% to 35%; and/or cellulose triacecate having a D.S. of 2 to 3 and an acetyl contact of 34% to 44.8%. More specifically, suitable cellulosic polymers include cellulose propionate having a D.S. of 1.8 and a propionyl content of 38.5%; cellulose acetate propionate having an acetyl content of 1.5% to 7% and a propionyl content of 39% to 42%; cellulose acetate propionate having an acetyl content of 2.5% to 3%, an average propionyl content of 39.2% to 45% and a hydroxyl content of 2.8% to 5.4%; cellulose acetate butyrate having a D. S. of 1.8, an acetyl content of 13% to 15% and a butyryl content of 34% to 39%; cellulose acetate butyrate having an acetyl content of 2% to 29.5%, a butyryl content of 17% to 53% and a hydroxyl content of 0.5% to 4.7%; cellulose triacylates having a D.S. of 2.9 to 3, such as cellulose trivalerate, cellulose trilaurate, cellulose tripalmitate, cellulose trioctanoate, and cellulose tripropionate; cellulose diesters having a D.S. of 2.2 to 2.6, such as cellulose disuccinate, cellulose dipalmitate, cellulose dioctanoate and cellulose dicarpylate; cellulose propionate morpholinbutyrate; cellulose acetate butyrate; cellulose acetate phthalate; mixed cellulose esters, such as cellulose acetate validate, cellulose acetate succinate, cellulose propionate succinate, cellulose acetate octanoate, cellulose valerate palmitate, cellulose acetate heptonate, and the like. Suitable semi-permeable polymers are disclosed in U.S. Pat. No. 4,077,407, which is incorporated herein by reference, and they can be made by procedures described in Encyclopedia of Polymer Science and Technology Vol. 3. pages 325–354, Interscience Publishers Inc., New York (1964).
Other suitable semi-permeable polymers include cellulose acetaldehyde, dimethyl cellulose acetate; cellulose acetate ethylcarbomate; cellulose acetate methylcarbomate; cellulose dimethylaminoacetate, a cellulose composition comprising cellulose acetate and hydroxypropylmethylcellulose; a composition comprising cellulose acetate and cellulose acetate butyrate; a cellulose composition comprising cellulose acetate butyrate and hydroxypropylmethylcellulose; semi-permeable polyamides; semi-permeable polyurethanes; semi-permeable polysulfanes; semi-permeable sulfonated polystyrene; crosslinked selectively semi-permeable polymers formed by the coprecipitation of a polyanion and a polycation as disclosed in U.S. Pat. Nos. 3,173,876, 3,276,586, 3,541,005, 3,541,006 and 3,546,142, all of which are incorporated herein by reference; selectively semi-permeable silicon rubbers; semi-permeable polymers as disclosed by Loeb and Sourirajan in U.S. Pat. No. 3,133,132, incorporated herein by reference, semi-permeable polystyrene derivatives; semi-permeable poly sodiumsytrenesulfonate); semi-permeable poly(vinylbenzyltrimethyl) ammonium chloride semi-permeable polymers exhibiting a fluid permeability of from 10−1 to 10−7 (cc.mil/cm2 hr-atm) expressed as per atmosphere of hydrostatic or osmotic pressure difference across a semi-permeable wall. The polymers are known to the art in U.S. Pat. Nos. 3,845,770, 3,916,899 and 4,160,020, all of which are incorporated herein by reference; and in J. R. Scott and W. J. Roff, Handbook of Common Polymers, CRC Press, Cleveland, Ohio, (1971).
The semi-permeable membrane is preferably supported in such a way that it is substantially inflexible such that its shape and position do not change as the expandable material expands. This is in order that the pressure generated in the system by the expandable material is not applied to the fluid source but instead to the product to be delivered.
Preferably, the aerosol delivery system includes a flexible impermeable membrane disposed between the pump and product to be delivered. For example, the flexible impermeable membrane might form a partition dividing the container into sub-chambers. As an alternative to a flexible impermeable membrane, the pump and product to be delivered may be separated by a piston.
In general, the impermeable membrane must be impermeable to water and the osmotically effective agent. Suitable impermeable materials include polyethylene, compressed polyethylene fine powder, polyethylene terephthalate (such as that marketed under the name Mylar), plasticized polyvinyl chloride, metal-foil polyethylene laminates, neoprene rubber, natural gum rubber and rubber hydrochloride such as that marketed under the name Pliofilm. These materials are preferably flexible, insoluble and chemically compatible with the product to be delivered. Additional suitable materials include polystyrene, polypropylene, polyvinyl chloride, reinforced epoxy resin, polymethylmethacrylate, or styrene/acrylonitrile copolymer.
The valve used in the aerosol delivery system according to the invention is optionally either manually operable or automatic. Where the valve is automatic, the pressure at which it operates is preferably variable. In general, a suitable automatic aerosol valve is a pressure actuated valve capable of releasing the compressed contents of a reservoir in stages as the contents of the reservoir reach a pre-determined internal pressure. A suitable activation pressure for the valve is from 2 to 10 atmospheres, preferably from 5 to 10 atmospheres, for example 7 atmospheres. With a low activation pressure of, for example, 2, 3 or 4 atmospheres a product can be delivered as a fine spray or stream. The shut off pressure for the automatic valve may be, for example, a pressure which is from 0.1 to 1 atmosphere less than the activation pressure or a pressure which is about 90% of the activation pressure.
Where the aerosol delivery system according to the invention is provided with a semi-permeable membrane, the membrane is preferably covered by a rupturable impermeable membrane. This is in order that the initial activation of the system can be controlled by the user. Optionally, the system is provided with means for rupturing the rupturable impermeable membrane, for example by making part of the container rotatable relative to the remainder.
A suitable container for use in the present invention is any conventionally used container which is able to withstand being pressurised. Suitable materials for making the container include metal or plastic materials, for example aluminium, tin plate, polyethylene terephthalate (PET), polyethylene naphalate (PEN) or a PET/PEN mixture, or glass particularly with a plastics safety layer.
A suitable product to be delivered by the system of the invention is, for example, a pesticide, herbicide, germicide, biocide, algicide, rodenticide, fungicide, insecticide, insect repellent, anti-oxidant, sterilant, plant growth promoter or inhibitor, preservative, anti-preservative, disinfectant, surface cleaning agent, enzyme digestant, air freshener, deodorant, antiperspirant, depilatory, antiseptic, polish, wax, odour neutraliser, laundry care agent, hair lacquer, topical skin treatment, catalyst, chemical reactant fermentation agent, food, food supplement, nutrient, cosmetic, drug, vitamin, sex sterilant, fertility inhibitor or promoter, air purifier, and/or microorganism attenuator. A suitable drug is any physiologically or pharmacologically active substance that produces a localised or systemic effect in a non-human animal, human, avian and/or domestic, recreational or farm animal. The drug may be administrable by topical, oral, nasal, opthalmic, rectal and/or vaginal means.
The fluid source is either provided from an external source or is within the container. The fluid source is preferably water.
The aerosol delivery system according to the invention can be activated either during manufacture or by the user when ready to use. For the system to be activated, the semi-permeable membrane of the expandable member needs to come into contact with a fluid source. The system may be activated: a) during manufacture, by the introduction of the external fluid to the pump device prior to aerosol device closure; or b) prior to first use by user, by introduction of an external fluid source; or removal of an internal seal.
The aerosol delivery system according to the invention can be activated to release the active agent either manually or by automatic action. The flow of the fluid from the fluid source to the pump may be controlled by modification of the semi-permeable membrane so that the time during which the system becomes repressurised following activation can be lengthened, if desired.
A further advantage of the invention is that it provides an aerosol delivery system which can be reactivated by the user.
For a better understanding of the invention and to show how the same may be carried into effect, reference will now be made, by way of example, to the accompanying drawings in which:
The above embodiments have been described by way of example only and many variations are possible without departing from the scope of the invention.
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|U.S. Classification||222/386, 141/20|
|International Classification||B65D83/14, B67D7/60|
|Nov 25, 2008||CC||Certificate of correction|
|Aug 27, 2010||FPAY||Fee payment|
Year of fee payment: 4
|Aug 27, 2014||FPAY||Fee payment|
Year of fee payment: 8